A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522219



Internal ID15449512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58345478..58347511hg38UCSC Ensembl
Innerchr11:58112951..58114984hg19UCSC Ensembl
Innerchr11:57869527..57871560hg18UCSC Ensembl
Innerchr11:57869527..57871560hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382034
hg192034
hg182034
hg172034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694996
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522219
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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